IACER Srl
22
MNPG338-00
Use only original spare parts supplied by the manufacturer; if non-original
spare parts are used, the operation and safety of the product might be affected
and the warranty will be null and void.
Interference and electromagnetic compatibility tables
The I-PRESS electrotherapy device is designed and built in compliance with
the current TECHNICAL STANDARD on ELECTROMAGNETIC COMPATIBILITY EN
60601-1-2:2015, with the aim of providing reasonable protection against
harmful interference in residential, civil and healthcare settings.
Based on their operating principle, the devices do not generate significant
radio frequency energy and have an adequate level of immunity to radiating
electromagnetic fields. Under these conditions, harmful interference cannot
occur to radioelectric communications and to the operation of electro-
medical devices used for monitoring, diagnosis, therapy and surgery, to the
operation of electronic office devices such as computers, printers, copiers,
faxes, etc. and to any electrical or electronic appliance used in such
environments, provided that they comply with the ELECTROMAGNETIC
COMPATIBILITY directive.
In any case, to prevent any problem with interference, it is recommended to
operate any therapy device at an appropriate distant from critical equipment
for monitoring patients' vital functions and to use caution in therapeutic
applications on patients with pacemakers. However, it is advisable to use the
device keeping a distance of at least 3 metres from televisions, monitors,
mobile phones or any other electronic equipment.
